ProBio
Head of Viral Vector Process Development
Head of Viral Vector Process Development
Get AI-powered advice on this job and more exclusive features. GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in gene and cell therapy (GCT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. Toward the mission of “Innovation through Collaboration”, GenScript ProBio is committed to helping customers shorten the timeline for the development of biological drugs from discovery to commercialization, significantly lowering R&D costs and building a healthier future. Report to: CEO of ProBio About the Role The position will lead the process development, optimization, and scale-up of viral vector manufacturing within the organization. And will manage a team of process development scientists and engineers, ensure robust and scalable production processes, and work closely with other departments to meet corporate objectives and regulatory standards Responsibilities Develop strategic plans for vector process development in alignment with organizational goals and regulatory requirements. Lead and drive the development of viral vector-based (e.g.lentivirus, retrovirus) manufacturing processes to improve efficiency, scalability, and product quality, with a focus on innovation and optimization. Design and oversee experiments to evaluate and improve viral vector production processes, utilizing statistical methods and experimental design principles. Manage the transfer of plasmid and viral vector processes from research and development to manufacturing, ensuring seamless integration and compliance with regulatory standards. Ensure all process development activities comply with relevant regulatory guidelines (FDA, EMA, etc.). Maintain rigorous quality control standards throughout the process development lifecycle. Prepare and review documentation for regulatory submissions and audits. Collaborate with manufacturing teams to troubleshoot and resolve production issues. Work closely with internal departments (e.g., Quality Assurance, Quality Control, Manufacturing) to align process development. Communicate project progress, challenges, and strategic plans to senior management and stakeholders. Represent the company at scientific conferences, industry meetings, and in publications. Stay abreast of industry trends and advancements to enhance ProBio's virus-related capabilities. Build and lead a high-performing global team focused on viral vector process development. Supervise a team of scientists and engineers engaged in process development activities, providing guidance, mentorship, and fostering a collaborative work environment. Strong analytical and problem-solving abilities, with a proactive approach to identifying and resolving technical challenges. Proven ability to collaborate effectively with cross-functional teams and external partners to achieve common objectives. Ability to thrive in a fast-paced, dynamic environment and adapt to changing priorities and requirements. Provide mentorship, guidance, and support to team members to foster professional growth. Qualifications B.S. and/or advanced degree in Chemical Engineering, Biochemistry, Virology and a relevant biological science field. Extensive industrial experience (Job level depends on experience) in viral vector process development and clinical manufacturing within the biopharmaceutical industry. In-depth knowledge of Lentiviral Vectors (LVV), and other viral vector technologies. Proven leadership experience with a track record of successfully leading global teams. Strong understanding of cGMP regulations and compliance in a manufacturing environment. Excellent written and verbal communication skills, with the ability to effectively communicate complex technical concepts to diverse audiences. Seniority level
Seniority level Director Employment type
Employment type Full-time Job function
Job function Science Industries Wholesale Drugs and Sundries Referrals increase your chances of interviewing at ProBio by 2x Sign in to set job alerts for “Head of Development” roles.
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Morristown, NJ $172,500.00-$249,166.66 9 hours ago Bedminster, NJ $160,000.00-$250,000.00 3 hours ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Head of Viral Vector Process Development
Get AI-powered advice on this job and more exclusive features. GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in gene and cell therapy (GCT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. Toward the mission of “Innovation through Collaboration”, GenScript ProBio is committed to helping customers shorten the timeline for the development of biological drugs from discovery to commercialization, significantly lowering R&D costs and building a healthier future. Report to: CEO of ProBio About the Role The position will lead the process development, optimization, and scale-up of viral vector manufacturing within the organization. And will manage a team of process development scientists and engineers, ensure robust and scalable production processes, and work closely with other departments to meet corporate objectives and regulatory standards Responsibilities Develop strategic plans for vector process development in alignment with organizational goals and regulatory requirements. Lead and drive the development of viral vector-based (e.g.lentivirus, retrovirus) manufacturing processes to improve efficiency, scalability, and product quality, with a focus on innovation and optimization. Design and oversee experiments to evaluate and improve viral vector production processes, utilizing statistical methods and experimental design principles. Manage the transfer of plasmid and viral vector processes from research and development to manufacturing, ensuring seamless integration and compliance with regulatory standards. Ensure all process development activities comply with relevant regulatory guidelines (FDA, EMA, etc.). Maintain rigorous quality control standards throughout the process development lifecycle. Prepare and review documentation for regulatory submissions and audits. Collaborate with manufacturing teams to troubleshoot and resolve production issues. Work closely with internal departments (e.g., Quality Assurance, Quality Control, Manufacturing) to align process development. Communicate project progress, challenges, and strategic plans to senior management and stakeholders. Represent the company at scientific conferences, industry meetings, and in publications. Stay abreast of industry trends and advancements to enhance ProBio's virus-related capabilities. Build and lead a high-performing global team focused on viral vector process development. Supervise a team of scientists and engineers engaged in process development activities, providing guidance, mentorship, and fostering a collaborative work environment. Strong analytical and problem-solving abilities, with a proactive approach to identifying and resolving technical challenges. Proven ability to collaborate effectively with cross-functional teams and external partners to achieve common objectives. Ability to thrive in a fast-paced, dynamic environment and adapt to changing priorities and requirements. Provide mentorship, guidance, and support to team members to foster professional growth. Qualifications B.S. and/or advanced degree in Chemical Engineering, Biochemistry, Virology and a relevant biological science field. Extensive industrial experience (Job level depends on experience) in viral vector process development and clinical manufacturing within the biopharmaceutical industry. In-depth knowledge of Lentiviral Vectors (LVV), and other viral vector technologies. Proven leadership experience with a track record of successfully leading global teams. Strong understanding of cGMP regulations and compliance in a manufacturing environment. Excellent written and verbal communication skills, with the ability to effectively communicate complex technical concepts to diverse audiences. Seniority level
Seniority level Director Employment type
Employment type Full-time Job function
Job function Science Industries Wholesale Drugs and Sundries Referrals increase your chances of interviewing at ProBio by 2x Sign in to set job alerts for “Head of Development” roles.
Duality- Head of Business Development and Strategic Alliances
Director, Business Development & Alliance
VP Business Development - Field Based - USA
Sr./Executive Director, Translational Research
Sr Director, Head of Corporate Affairs, Global R&D and Business Development
The Head of EGDS Innovation and Center of Excellence
Morristown, NJ $258,750.00-$373,750.00 1 week ago Newark, NJ $185,100.00-$250,500.00 3 days ago Senior Director, TPM TA Head Immunology and Immuno-oncology
East Hanover, NJ $248,500.00-$461,500.00 2 weeks ago Bridgewater, NJ $170,000.00-$200,000.00 2 weeks ago Director of Business Development - Custom API/Intermediate CDMO
Head of Immunology Development Operations
Morristown, NJ $172,500.00-$249,166.66 6 hours ago Rahway, NJ $169,700.00-$267,200.00 3 weeks ago Associate Director/Director of PV Operations
Senior Director, Internal Consulting Team
Senior Director, Internal Consulting Team
Cranbury, NJ $308,000.00-$369,000.00 6 days ago Clinical Development Program Lead, Neuropsychiatry (Executive Director)
Executive Director - Therapeutic Area Operations Leader- Obesity, Muscle, Metabolism
Business Development Executive - Telecommunications
New Jersey, United States $140,000.00-$185,000.00 1 week ago Allendale, NJ $160,000.00-$225,000.00 1 day ago Clinical Development Program Lead, Neuropsychiatry (Executive Director)
Head of Immunology Development Operations
Morristown, NJ $172,500.00-$249,166.66 9 hours ago Bedminster, NJ $160,000.00-$250,000.00 3 hours ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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